Rett syndrome – biological pathways leading from MECP2 to disorder phenotypes

Overview of attention for article published in Orphanet Journal of Rare Diseases, November 2016

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Mentioned by

twitter: 6 X users

wikipedia: 3 Wikipedia pages

Citations

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mendeley: 245 Mendeley
citeulike: 2 CiteULike

Summary X Wikipedia Dimensions citations

So far, Altmetric has seen 3 citations on 3 Wikipedia pages.

Uzbek

Rett sindromi

Cited by user Riki Puch on 06 Aug 2022

Rett sindromi (RTT) irsiy kasallik boʻlib, odatda ayollarda 6-18 oylikdan keyin namoyon boʻladi.

Arabic

متلازمة ريت

Cited by user عبد الله عرفة (بيت الحكمة) on 19 Feb 2022

English

Rett syndrome

Cited by user Egon Willighagen on 24 Feb 2017

Rett syndrome (RTT), originally termed cerebroatrophic hyperammonemia, is a rare genetic postnatal neurological disorder of the grey matter of the brain that almost…

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